Supervisor Quality Control Microbiology
for section headings. Use - for any list of duties/requirements/benefits. Use
for prose.
Thus:
About the role
We are currently looking to fill a 2nd shift Quality Control Supervisor focused in Microbiology. Our Quality Control Microbiology Department is responsible for activities related to pharmaceutical microbiology including environmental, personnel and utility monitoring, raw material, in-process, and product release testing. This position will be responsible for ensuring daily operations are completed accurately, timely, and reliably to ensure our medicines are safe and effective before reaching patients around the world. This is an excellent opportunity to join a select group of colleagues while working on molecules that help improve patients lives.
Responsibilities
- Coordinate testing and monitoring activities within the QC lab and manufacturing facility.
- Review test results, procedures, protocols, and quality system records.
- Attend cross-functional meetings to remain informed of business needs.
- Organize lab investigations and assay troubleshooting as needed.
- Support internal and regulatory audits.
- Ensure safety and current Good Manufacturing Practice standards are maintained.
- Execute personnel management functions including performance evaluations, personnel development, and scheduling time off.
- Communicate effectively with management on complex matters; support laboratory management in mid to long range team goals.
- Drive and manage projects within the group.
- Coach team members in troubleshooting microbiology methods, Environmental Monitoring, aseptic techniques and equipment.
Requirements
A BS/BA in Life Sciences or related field, with 5+ years of progressive, relevant experience, preferably within pharmaceutical microbiology. Supervisory/leadership experience required.
Benefits
- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Insurance benefits (e.g. medical, dental, vision, life and disability)
- Paid time off
- Family support benefits
Pay
Salary Range (annually) $78,700.00 - $128,700.00
Schedule
2nd shift Tuesday‑Saturday, 2 PM – 10:30 PM
Check for any missing substantive info: Location: Rensselaer, New York, United States. Should we include location? It's substantive. Where to put? Could be part of About the role or maybe a separate section? There's no heading for Location; but we could include it in About the role paragraph. Add location after intro. Let's incorporate: "Location: Rensselaer, New York, United States." So modify About the role paragraph to include that.
Also note "When & Where 2nd shift Tuesday- Saturday, 2 PM - 10:30 PMLocation: Rensselaer, New York, United States" we already captured shift in Schedule and location in About.
Thus About the role paragraph: "We are currently looking to fill a 2nd shift Quality Control Supervisor focused in Microbiology. Our Quality Control Microbiology Department is responsible for activities related to pharmaceutical microbiology including environmental, personnel and utility monitoring, raw material, in-process, and product release testing. This position will be responsible for ensuring daily operations are completed accurately, timely, and reliably to ensure our medicines are safe and effective before reaching patients around the world. This is an excellent opportunity to join a select group of colleagues while working on molecules that help improve patients lives. Location: Rensselaer, New York, United States."
Check for any other substantive info: "Discover Your Role" heading is just a heading; we already used Responsibilities.
Anything about "Must be able to work 2nd shift Tuesday- Saturday, 2 PM - 10:30 PM" we placed in Schedule.
Anything about "Supervisory/leadership experience required." we placed in Requirements.
Anything about "BS/BA in Life Sciences or related field, with 5+ years of progressive, relevant experience, preferably within pharmaceutical microbiology." we placed in Requirements.
Anything about "Coordinate testing and monitoring activities within the QC lab and manufacturing facility." etc we have.
Anything about "Review test results, procedures, protocols, and quality system records." etc.
Anything about "Attend cross-functional meetings to remain informed of business needs." etc.
Any
for prose. Thus:
About the role
We are currently looking to fill a 2nd shift Quality Control Supervisor focused in Microbiology. Our Quality Control Microbiology Department is responsible for activities related to pharmaceutical microbiology including environmental, personnel and utility monitoring, raw material, in-process, and product release testing. This position will be responsible for ensuring daily operations are completed accurately, timely, and reliably to ensure our medicines are safe and effective before reaching patients around the world. This is an excellent opportunity to join a select group of colleagues while working on molecules that help improve patients lives.
Responsibilities
- Coordinate testing and monitoring activities within the QC lab and manufacturing facility.
- Review test results, procedures, protocols, and quality system records.
- Attend cross-functional meetings to remain informed of business needs.
- Organize lab investigations and assay troubleshooting as needed.
- Support internal and regulatory audits.
- Ensure safety and current Good Manufacturing Practice standards are maintained.
- Execute personnel management functions including performance evaluations, personnel development, and scheduling time off.
- Communicate effectively with management on complex matters; support laboratory management in mid to long range team goals.
- Drive and manage projects within the group.
- Coach team members in troubleshooting microbiology methods, Environmental Monitoring, aseptic techniques and equipment.
Requirements
A BS/BA in Life Sciences or related field, with 5+ years of progressive, relevant experience, preferably within pharmaceutical microbiology. Supervisory/leadership experience required.
Benefits
- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Insurance benefits (e.g. medical, dental, vision, life and disability)
- Paid time off
- Family support benefits
Pay
Salary Range (annually) $78,700.00 - $128,700.00
Schedule
2nd shift Tuesday‑Saturday, 2 PM – 10:30 PM
Check for any missing substantive info: Location: Rensselaer, New York, United States. Should we include location? It's substantive. Where to put? Could be part of About the role or maybe a separate section? There's no heading for Location; but we could include it in About the role paragraph. Add location after intro. Let's incorporate: "Location: Rensselaer, New York, United States." So modify About the role paragraph to include that. Also note "When & Where 2nd shift Tuesday- Saturday, 2 PM - 10:30 PMLocation: Rensselaer, New York, United States" we already captured shift in Schedule and location in About. Thus About the role paragraph: "We are currently looking to fill a 2nd shift Quality Control Supervisor focused in Microbiology. Our Quality Control Microbiology Department is responsible for activities related to pharmaceutical microbiology including environmental, personnel and utility monitoring, raw material, in-process, and product release testing. This position will be responsible for ensuring daily operations are completed accurately, timely, and reliably to ensure our medicines are safe and effective before reaching patients around the world. This is an excellent opportunity to join a select group of colleagues while working on molecules that help improve patients lives. Location: Rensselaer, New York, United States." Check for any other substantive info: "Discover Your Role" heading is just a heading; we already used Responsibilities. Anything about "Must be able to work 2nd shift Tuesday- Saturday, 2 PM - 10:30 PM" we placed in Schedule. Anything about "Supervisory/leadership experience required." we placed in Requirements. Anything about "BS/BA in Life Sciences or related field, with 5+ years of progressive, relevant experience, preferably within pharmaceutical microbiology." we placed in Requirements. Anything about "Coordinate testing and monitoring activities within the QC lab and manufacturing facility." etc we have. Anything about "Review test results, procedures, protocols, and quality system records." etc. Anything about "Attend cross-functional meetings to remain informed of business needs." etc. Any